Canonical Allele Identifier: PA2825218577
Gene: ATP2B4 HGNC NCBI
ClinVar RCV:
RCV001896647
ClinVar Variation:
1400320
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001396.1:p.Arg474His
CA344314192
NM_001001396.3:c.1421G>A